Literature DB >> 27748512

Genetics of mitochondrial dysfunction and infertility.

L A M Demain1,2, G S Conway3,4, W G Newman1,2.   

Abstract

Increasingly, mitochondria are being recognized as having an important role in fertility. Indeed in assisted reproductive technologies mitochondrial function is a key indicator of sperm and oocyte quality. Here, we review the literature regarding mitochondrial genetics and infertility. In many multisystem disorders caused by mitochondrial dysfunction death occurs prior to sexual maturity, or the clinical features are so severe that infertility may be underreported. Interestingly, many of the genes linked to mitochondrial dysfunction and infertility have roles in the maintenance of mitochondrial DNA or in mitochondrial translation. Studies on populations with genetically uncharacterized infertility have highlighted an association with mitochondrial DNA deletions, whether this is causative or indicative of poor functioning mitochondria requires further examination. Studies on the impact of mitochondrial DNA variants present conflicting data but highlight POLG as a particularly interesting candidate gene for both male and female infertility.
© 2016 John Wiley & Sons A/S. Published by John Wiley & Sons Ltd.

Entities:  

Keywords:  POLG; infertility; mitochondria; primary ovarian insufficiency

Mesh:

Substances:

Year:  2016        PMID: 27748512     DOI: 10.1111/cge.12896

Source DB:  PubMed          Journal:  Clin Genet        ISSN: 0009-9163            Impact factor:   4.438


  26 in total

1.  Mitochondrial DNA copy number in peripheral blood: a potential non-invasive biomarker for female subfertility.

Authors:  Andrea Busnelli; Debora Lattuada; Raffaella Rossetti; Alessio Paffoni; Luca Persani; Luigi Fedele; Edgardo Somigliana
Journal:  J Assist Reprod Genet       Date:  2018-08-17       Impact factor: 3.412

Review 2.  Mitochondrial dynamics during spermatogenesis.

Authors:  Grigor Varuzhanyan; David C Chan
Journal:  J Cell Sci       Date:  2020-07-16       Impact factor: 5.285

Review 3.  Genetics of human female infertility†.

Authors:  Svetlana A Yatsenko; Aleksandar Rajkovic
Journal:  Biol Reprod       Date:  2019-09-01       Impact factor: 4.285

Review 4.  Mitochondrial Dysfunction in Primary Ovarian Insufficiency.

Authors:  Dov Tiosano; Jason A Mears; David A Buchner
Journal:  Endocrinology       Date:  2019-10-01       Impact factor: 4.736

5.  Incompatibility between mitochondrial and nuclear genomes during oogenesis results in ovarian failure and embryonic lethality.

Authors:  Chunyang Zhang; Kristi L Montooth; Brian R Calvi
Journal:  Development       Date:  2017-06-02       Impact factor: 6.868

6.  Mutations in VPS13D lead to a new recessive ataxia with spasticity and mitochondrial defects.

Authors:  Eunju Seong; Ryan Insolera; Marija Dulovic; Erik-Jan Kamsteeg; Joanne Trinh; Norbert Brüggemann; Erin Sandford; Sheng Li; Ayse Bilge Ozel; Jun Z Li; Tamison Jewett; Anneke J A Kievit; Alexander Münchau; Vikram Shakkottai; Christine Klein; Catherine A Collins; Katja Lohmann; Bart P van de Warrenburg; Margit Burmeister
Journal:  Ann Neurol       Date:  2018-06-30       Impact factor: 10.422

7.  Maternal age at birth and daughter's fecundability.

Authors:  Olga Basso; Sydney K Willis; Elizabeth E Hatch; Ellen M Mikkelsen; Kenneth J Rothman; Lauren A Wise
Journal:  Hum Reprod       Date:  2021-06-18       Impact factor: 6.918

Review 8.  Mitochondrial Dysfunction in Obesity and Reproduction.

Authors:  Manasi Das; Consuelo Sauceda; Nicholas J G Webster
Journal:  Endocrinology       Date:  2021-01-01       Impact factor: 5.051

9.  Mitochondrial DNA sequencing and large-scale genotyping identifies MT-ND4 gene mutation m.11696G>A associated with idiopathic oligoasthenospermia.

Authors:  Juan Ji; Miaofei Xu; Zhenyao Huang; Lei Li; Hongxiang Zheng; Shuping Yang; Shilin Li; Li Jin; Xiufeng Ling; Yankai Xia; Chuncheng Lu; Xinru Wang
Journal:  Oncotarget       Date:  2017-05-08

Review 10.  Recent developments in genetics and medically assisted reproduction: from research to clinical applications.

Authors:  J C Harper; K Aittomäki; P Borry; M C Cornel; G de Wert; W Dondorp; J Geraedts; L Gianaroli; K Ketterson; I Liebaers; K Lundin; H Mertes; M Morris; G Pennings; K Sermon; C Spits; S Soini; A P A van Montfoort; A Veiga; J R Vermeesch; S Viville; M Macek
Journal:  Eur J Hum Genet       Date:  2017-12-04       Impact factor: 4.246

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